美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA090162"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
80425-0576-1 80425-0576 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA090162 Advanced Rx of Tennessee, LLC TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-1)
80425-0576-2 80425-0576 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA090162 Advanced Rx of Tennessee, LLC TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-2)
80425-0576-3 80425-0576 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA090162 Advanced Rx of Tennessee, LLC TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-3)
80425-0576-4 80425-0576 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA090162 Advanced Rx of Tennessee, LLC TOPIRAMATE 25 mg/1 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-4)
71335-1064-0 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1064-0)
71335-1064-1 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1064-1)
71335-1064-2 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190111 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1064-2)
71335-1064-3 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190115 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1064-3)
71335-1064-4 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1064-4)
71335-1064-5 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190131 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-1064-5)
71335-1064-6 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 80 TABLET, FILM COATED in 1 BOTTLE (71335-1064-6)
71335-1064-7 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190531 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1064-7)
71335-1064-8 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-1064-8)
71335-1064-9 71335-1064 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-1064-9)
72162-2480-0 72162-2480 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2480-0)
72162-2480-5 72162-2480 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2480-5)
72162-2480-6 72162-2480 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA090162 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72162-2480-6)
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